← Back to catalogue

Bracket Pro Series

EUDAMED

Class I (EU MDR)

Ref 552-10-AB-BR, 320-10-PRO-RDT, 320-10-PRO-RDT-SMT, 321-10-LS-RDT-SMT 321-10-LS-RDT, 320-12-PRO-ND

by Technimount E.M.S. Holding inc.

Identity

Trade Name
Bracket Pro Series EUDAMED
Device Name
Bracket Pro series mounts EUDAMED
Model / Reference
552-10-AB-BR, 320-10-PRO-RDT, 320-10-PRO-RDT-SMT, 321-10-LS-RDT-SMT 321-10-LS-RDT, 320-12-PRO-ND EUDAMED

Identifiers

Primary DI / UDI-DI
00628678604025 EUDAMED
Basic UDI-DI
628678604001JK EUDAMED
EMDN Code
V0880 MEDICAL SUPPORT EQUIPMENT - ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Bracket Pro Series by Technimount E.M.S. Holding inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CA-MF-000038672
Authorised Representative
Arazy Group (Ireland) Ltd. IE-AR-000000093

Sources (2)

  • EUDAMED 7836dad9-33a3-47f8-8072-58e2bdc51b32 61 fields · synced Jul 29, 2026
  • EUDAMED 7836dad9-33a3-47f8-8072-58e2bdc51b32-1 61 fields · synced Jun 9, 2026